|Número de publicación||US7282232 B2|
|Tipo de publicación||Concesión|
|Número de solicitud||US 10/451,808|
|Número de PCT||PCT/GB2002/000165|
|Fecha de publicación||16 Oct 2007|
|Fecha de presentación||17 Ene 2002|
|Fecha de prioridad||19 Ene 2001|
|También publicado como||EP1368536A1, US20040096554, WO2002057545A1|
|Número de publicación||10451808, 451808, PCT/2002/165, PCT/GB/2/000165, PCT/GB/2/00165, PCT/GB/2002/000165, PCT/GB/2002/00165, PCT/GB2/000165, PCT/GB2/00165, PCT/GB2000165, PCT/GB200165, PCT/GB2002/000165, PCT/GB2002/00165, PCT/GB2002000165, PCT/GB200200165, US 7282232 B2, US 7282232B2, US-B2-7282232, US7282232 B2, US7282232B2|
|Inventores||John Edward Rose, Glynn Arthur Wardle|
|Cesionario original||John Edward Rose, Glynn Arthur Wardle|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citas de patentes (10), Otras citas (1), Clasificaciones (19), Eventos legales (4)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
The present invention relates to a bonded fibrous sheet material which is useful, for example, in the manufacture of casings (e.g. skins) for food products.
It is well known that number of food products (particularly certain meat products) are, during their process of manufacture, enclosed within a skin which retains the form or shape of the product. Examples of such food products are sausages, salami etc.
One method which has been used extensively for producing such casings involves viscose treatment of a porous paper web, as described more fully in U.S. Pat. No. 3,135,613. Briefly this process involves the steps of
(a) forming a bonded fibrous web by treatment of the paper with a dilute viscous solution (to apply approximately 1-3% of viscose based on the weight of the paper), drying the web, regenerating cellulose by acid treatment, washing and further drying. The product of this step is a porous, bonded fibrous web having sufficient caustic resistance to withstand the highly alkaline conditions of step (b). Conventionally step (a) has been carried out by the manufacturer of the paper; and
(b) treating the bonded web obtained from step (a) with a highly caustic viscose solution (to apply 300%-400% of viscose by weight of the paper), followed by regeneration of cellulose and washing and drying steps to produce the food casing material.
The product of step (a) has properties rendering it highly desirable for use as a food casing. More particularly, the casings are:
1. porous and permeable to moisture vapor and smoke thus allowing food products enclosed therein to be processed;
2. dimensionally stable to allow food products which may for example be salami of substantial lengths and relatively heavy to be hung without losing their shape; and
3. clear to the extent that the fibrous base cannot be seen.
Such casings are perfectly satisfactory and have been used for many years. However step (1) does have processing disadvantages in that it is a multi-stage process involving dope addition, acidification, neutralisation and washing stages. The multi-stage process associated with step (3) is an accepted process requirement in the industry and is not seen as a particular disadvantage.
Various patents have discussed the use of alternative materials for bonding paper webs to provide an appropriate substrate for casing forming operations where treatment with concentrated viscose solution under highly alkaline conditions is carried out. After undergoing bonding the substrate must retain its porous, absorbent characteristics in order to permit adequate impregnation and encasement by the converted viscose. The bonding agent should also be one that will not cause the substrate to become discoloured during exposure to the conditions of the casing forming process.
U.S. Pat. No. 3,484,256 (Chiu et al) suggests cationic thermosetting resin and polyacrylamide as a replacement for the dilute viscose bonding treatment. U.S. Pat. No. 3,640,734-5 (Conway), and U.S. Pat. No. 3,679,437 (Oppenheimer et al) teach the use of soluble poly (vinyl alcohol) as a wet strengthening agent.
The aforementioned binder materials, whether used alone or in combination frequently provide some but not all of the desired characteristics of the casing. For example the use of poly (vinyl alcohol) having a degree of hydrolysis of about 85% will provide low to moderate dry tensile strengths but poor wet tensile, caustic strength and absorption characteristics. Conversely, the use of fibrous film forming materials such as hydroxyethyl cellulose in conjunction with appropriate cross linking agent such as dialdehyde cross linkers will have the opposite effect from that achieved by the poly(vinyl alcohol). They exhibit good wet tensile strengths and absorbency characteristics but poor caustic tensile strength. Unfortunately, mixtures of these materials also fail to provide all the desired characteristics.
JP-A-6294094 (Oji Paper Co) discloses manufacture of a paper which is stated to have good wet strength and good alkali resistance and which is suitable for use as a casing for a meat product (e.g. ham or sausage) or in the manufacture of tea bags. The paper is produced by adding guar gum and a polyamide epichlorohydrin resin (a wet strength agent) to the wet end of the paper making process. We have however found that papers using this technique do not actually have sufficient wet tensile strength and caustic tensile strength for consistent conversion to food casing material in step (b) outlined above.
WO-A-9510190 (J. R. Crompton Limited) discloses a bonding fibrous sheet material suitable for conversion, by viscose treatment, into a food casing material. The bonded fibrous sheet material is produced by treatment of a porous fibrous substrate (particularly a paper) with a coating composition which under the conditions of the treatment does not form a film and which is an admixture of a polymer latex and a wet strength resin, and effecting cross-linking of the polymer and resin to produce the porous bonded, fibrous sheet material. It is contemplated in WO-A-9510190 that the coating composition may include a fibre consolidation aid, e.g. in an amount of less than 3% by weight of the coating composition. The preferred fibre consolidation aid is carboxymethyl cellulose and other examples given include galactomannan, e.g. guar gum and locust bean gum. We have however found that this binder system can still cause fracture lines and poor body penetration if the latex component is over or under cured. Furthermore, preferred impregnants in accordance with WO-A-9510190 include a surfactant (in addition to the latex and wet-strength resin) and if the surfactant level is not correctly controlled in the impregnant then there is an adverse impact on fracture line propagation.
It is therefore an object of the present invention to obviate or mitigate the above mentioned disadvantages and provide a method of producing a bonded web having characteristics associated with dilute viscose bonded materials.
According to a first aspect of the present invention there is provided a method of producing a porous bonded fibrous sheet material comprising
(i) treating a porous fibrous substrate which is comprised of cellulosic fibres and which has a moisture content of less than 10% by weight with a gum and a cross-linkable wet strength resin both dissolved in water, said treatment being effected otherwise than with a latex;
(ii) removing excess water; and
(iii) effecting cross-linking of the resin.
According to a second aspect of the present invention there is provided a porous bonded fibrous sheet material produced by the method of the first aspect of the invention.
The porous fibrous substrate will generally be a wet-laid material, particularly a paper. The paper (or other porous fibrous substrate) to be treated has a moisture content of less than 10% by weight, more preferably less than 5%, e.g. 3-5%, and as such is generally referred to in the industry as being “bone-dry” (although it does contain the indicated amount of moisture). We have found that use of a gum and a wet strength resin to treat the “dry” (i.e. less than 10% moisture) porous fibrous substrate provides a bonded material having significantly improved wet tensile strength and caustic tensile strength as compared to a material produced by a wet-laying process involving addition of a gum and a wet strength resin only at the wet end of the process (i.e. as disclosed in JP-A-6294094). Whilst we do not wish to be bound by theory we believe that during cross-linking of the wet strength resin both the gum and the cellulose (of the fibres) are also involved in cross-linking. As a result, the wet-strength resin, the gum and the cellulose are cross-linked together and it is this cross-linking which provides the improved properties for the bonded material. Surprisingly also the properties of the material (in accordance with the second aspect of the invention) are improved compared to those obtained with the procedure of WO-A-9510190, even though a much simplified binding system is used (i.e. without latex). Compared to the preferred materials of WO-A-9510190, materials produced in accordance with the invention typically have in total dry tensile, total wet tensile and total caustic tensile of 29%, 23% and 33% respectively. Materials in accordance with the invention also have much improved absorbency.
Bonded fibrous sheet materials in accordance with the second aspect of the invention are eminently suitable for conversion into a food casing material by a viscose treatment (i.e. step (b) above) as employed in the prior art conversions of viscose pre-treated paper or any other suitable material.
Therefore according to a third aspect of the present invention there is provided a food casing material which comprises the bonded fibrous sheet material in accordance with the second aspect of the invention treated with viscose.
Typically the food casing material will comprise 300%-400% of viscose by weight of the base porous substrate.
Food casing materials produced in accordance with the third aspect of the invention meet requirements (1)-(3) above. Furthermore the bonding which is achieved between the viscose and the cross-linked coating composition results in lower levels of stress line fracture normally associated with resin bonded casing substrates. Additionally the food casing materials have improved stretch characteristics and casing clarity when compared to other resin bonded systems, with the resultant clarity being comparable to that of materials obtained using viscose pre-treated substrates.
According to a fourth aspect of the present invention there is provided a food product (e.g. a meat product such as a sausage or salami) enclosed within a food casing material in accordance with the third aspect of the invention.
In addition to its use in the manufacture of food casing materials, the bonded web material of the invention may be used in the production of beverage filtration products, e.g. tea bags, coffee bags etc. The material is also useful in the production of sachets for washing powders and double-sided adhesive tapes.
In practising the method of the first aspect of the invention, the porous fibrous substrate will preferably be treated with an aqueous solution which contains both the gum and the cross-linkable wet strength resin dissolved in water. We do not however preclude the possibility of treating the substrate with separate solutions of the gum and the resin. The solution(s) applied to the fibrous substrate is/are non-film forming (under the conditions of treatment) to ensure that the bonded material ultimately obtained is porous.
Preferably the total amount of the gum and wet strength resin applied to the porous fibrous substrate is less than 10% (e.g. 1 to 10%) by weight of the untreated substrate. Typically the amount of the wet strength resin applied to the substrate will be less than 5%, usually 0.05-2%, by weight of the untreated substrate. Typically also the amount of gum applied to the substrate will be 0.05%-3% on the same weight basis.
Preferably the gum is non-ionic. Preferably the gum is a galactomannan gum and is most preferably unsubstituted. The gum will generally be a vegetable gum. Examples of gums that may be used in the present invention include guar gum and locust bean gum which are widely used as formation aids in paper making processes by addition to the wet end of the process.
A range of wet strength resins may be used. If however it is intended that the final precursor material be subsequently treated with viscose to produce the finished food casing then the final wet strength system should be alkali resistant.
Suitable wet strength resins are water soluble cationic epichlorohydrin polyamide products, e.g. Kymene 709 as available from Hercules Ltd. which becomes alkali resistant in combination with the gum (Kymene is a Registered Trade Mark).
Preferably the porous substrate is a wet laid fibrous substrate, most preferably a paper. Most preferably the paper is of a high and uniform permeability (preferably 100-200 m3 min−1 m−2) and of low basis weight (typically 10-30 gsm). Preferably also the paper has a tensile ratio (i.e. ratio of machine direction:cross direction strength) of 0.5-2.0 more preferably in the range 1.0-1.5. The paper is ideally prepared from “long” fibres (e.g. 5 mm) of high aspect ratio (e.g. 300-3000). The web's constituent fibres should also exhibit uniform formation and absorbency characteristics. Particularly suitable papers are composed entirely of natural cellulosic fibres typically of the Musa Textilis species (e.g. Abaca). It is also possible to use papers comprised partially of synthetic fibres.
Preferred papers for use (as the porous fibrous substrate) to be treated in accordance with the first aspect of the invention are manufactured with the addition of a gum and a wet strength resin to the wet end of the paper making process (in addition to the gum and wet strength resin applied to the “dry” paper). The amount of gum included in the as-manufactured paper (i.e. prior to treatment in accordance with the first aspect of the invention) is preferably 0.5% to 2.5% by weight and the amount of wet strength resin in the “as-manufactured” paper is preferably 0.3% to 1.5%.
In the case where the porous fibrous substrate to be treated in accordance with the first aspect of the invention is a paper then such treatment may be effected after drying of the paper web (formed on the paper making fabric or wire) to a moisture content of less than 10% (typically 3-5%) as conventionally happens in paper manufacture. The treatment is conveniently effected by application of a solution comprising the gum and the wet strength resin by means of a size press although other methods of impregnating the substrate may be used, e.g. spraying or immersion. In any such treatment, the amount of the solution applied to the web will be controlled so that, after drying, the required amount of gum and wet strength resin remain on the paper.
Drying of the paper that has been treated with the solution (containing the gum and wet strength resin) may be effected using a drying cylinder, through air/float air dryer of the like.
Cross-linking of the wet-strength resin may be effected by heating, typically to a temperature above 100° C., usually 200-300° C. and typically 220-250° C.
The invention will be illustrated with reference to the following non-limiting Examples and
An Abaca paper was produced on a pilot papermaking machine. The paper had an Abaca paper having a basis weight of about 23.5 gsm (average fibre length ca 5 mm, aspect ratio 300-3000), a moisture content of about 4% by weight and contained 0.5% by weight Kymene and 2% by weight guar gum (ex Rhodia) incorporated during wet-laying.
The paper was then size pressed with an aqueous solution comprising
1Guar Gum (ex Rhodia)
Kymene 709 (ex Hercules)
(1Meypro Guar CSA 200/50).
The size press was adjusted so that the paper was impregnated with its own weight of the coating composition (solids content 0.75%).
The paper was dried to a moisture content of about 4% using a combination of drying cylinder and through air drying methods on the pilot papermaking machine and was then heated to a temperature of 150° C. by an air flotation curing oven to cure the binder system. The physical properties of the web thus obtained are listed in Table 1.
2Total Wet Tensile g/15 mm
2Total Caustic Tensile g/15 mm
2MD:CD = ca 1.5
The value for wet tensile strength and caustic tensile strength compare with values of 198-432 g/15 mm and 61-120 g/15 mm respectively as obtained in Examples 1-3 of JP-A-6294094 (Oji Paper Co.) where Guar Gum and polyamide epichlorohydrin are only added to the wet end of the paper making process.
Example 1 was repeated save that the paper was size pressed with the following solution:
Guar Gum (ex Rhodia)
0.5% by weight
Kymene 709 (ex Hercules)
0.9% by weight
The properties of the material obtained are shown in Table 2.
2Wet Tensile g/15 mm
2Caustic Tensile g/15 mm
2MD:CD = ca 1.5
This test was carried out on the following paper samples:
(i) the paper of Example 2;
(ii) an Abaca paper having a viscose binder;
(iii) an Abaca paper having a poly(vinyl alcohol).
An A4 sample of the paper was taken and a base line drawn 2″ from the bottom of the sample in portrait orientation. On this line roughly 4 inches to the left of centre of the sheet a small vertical line was made and marked as COAG. The same mark was made to the right of the centre and marked as REGEN.
The sample was then laid flat on a glass plate and using a circa 2 mm coating bar a concentrated viscose solution was laid evenly across the sample.
The sample was carefully transferred to a bath containing the coagulant chemicals (typically sulphuric acid, sodium sulphate and ammonium sulphite) at a strength to achieve ca 60% regeneration and left for 30 seconds to start initial coagulation. The sample was then carefully folded along the COAG mark so as to place the viscose coated faces together. The fold was then reinforced by running a standard ink spreading roller up and down the fold three times. The sample was then laid flat again in the COAG bath for a further 2.5 minutes to finish coagulation.
The sample was then carefully transferred to the regeneration chemical bath (sulphuric acid) at a strength sufficient to achieve 99% regeneration and left for 30 seconds. The above folding and pressing action was carried out on the REGEN marked line and the sample left for 2.5 minutes to finish regenerating.
The sample was rinsed under running water for 20 minutes to neutralise the chemicals, placed in a 10% gylcerol solution bath for 10 minutes and finally stretched between two standard embroidery hoops.
The stretched samples were then dried in a standard laboratory oven until dry at 105° C.
The samples were reverse mounted (viscose on back of sheet) to exemplify any stress fracture lines caused and/or body penetration issues.
The results of the tests are shown in
It will be seen that no fracture lines developed in paper (i) (i.e. a paper in accordance with the invention) which emulated a paper (ii), i.e. one with typical viscose binder system. In contrast, paper (iii) (which utilised a non-viscose binder, i.e. poly(vinyl alcohol)) gave fracture lines.
The test was conducted using a Paprical Bristow dynamic sorption unit supplied by Optest Equipment Inc. of Canada.
The test equipment utilises the Lucas Washburn theory of the rate of sorption of water into a porous structure of paper, which should be proportional to the square-root of the time available for sorption.
This test was carried out on the following samples of paper:
(iv) a dialdehyde bonded paper;
(v) a first poly(vinyl alcohol) bonded paper;
(vi) a second poly (vinyl alcohol) bonded paper;
(vii) the paper of Example 2;
(viii) a viscose bonded paper.
The absorbency of each paper was determined by using the above equipment to evaluate the samples penetration by a viscose solution of a particular viscosity (3850 cp) over a range of application speeds measured in milliseconds. The results are shown in
Furthermore, the test was carried out on paper (vii) (i.e. the paper in accordance with the invention) for a range of viscose solutions of different viscosity each at a range of application speeds. The results are shown in
|Patente citada||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US4207353 *||21 Feb 1979||10 Jun 1980||Union Carbide Corporation||Food casing and method of preparing same|
|US4299654 *||31 Dic 1979||10 Nov 1981||Ciba-Geigy Corporation||Process for producing sized paper and cardboard with polyelectrolytes and epoxide-amine-polyamide reaction products|
|US5690790 *||28 Mar 1996||25 Nov 1997||The Procter & Gamble Company||Temporary wet strength paper|
|US5718804 *||3 Oct 1995||17 Feb 1998||Bayer Aktiengesellschaft||Process for the production of cellulose-containing sheet-like structures which have been given a dry strength and/or wet strength treatment|
|US5912306 *||22 Nov 1996||15 Jun 1999||Hercules Incorporated||Cationic compounds useful as drainage aids and stabilizers for rosin-based sizing agents|
|US6319361 *||12 May 2000||20 Nov 2001||The Procter & Gamble Company||Paper products having wet strength from aldehyde-functionalized cellulosic fibers and polymers|
|US6582559 *||4 May 2001||24 Jun 2003||Sca Hygiene Products Zeist B.V.||Aldehyde-containing polymers as wet strength additives|
|US6896725 *||25 Abr 2003||24 May 2005||Sca Hygiene Products Zeist B.V.||Aldehyde-containing polymers as wet strength additives|
|WO1995010190A1 *||10 Oct 1994||20 Abr 1995||Judith Cormack||Bonded fibrous sheet material|
|WO1999034058A1 *||30 Dic 1998||8 Jul 1999||Hercules Inc||Oxidized galactose type of alcohol configuration containing polymer in combination with cationic polymers for paper strength applications|
|Clasificación de EE.UU.||426/135, 428/36.5, 162/164.3, 162/207, 428/36.4, 426/138, 426/105|
|Clasificación internacional||D21H21/20, D21H17/55, D21H17/31, A23P1/08, D21H25/06|
|Clasificación cooperativa||Y10T428/1372, Y10T428/1376, D21H21/20, D21H17/31, D21H17/55, D21H25/06|
|21 Oct 2003||AS||Assignment|
Owner name: J R CROMPTON LIMITED, GREAT BRITAIN
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:ROSE, JOHN EDWARD;WARDLE, GLENN A.;REEL/FRAME:014931/0916
Effective date: 20030708
|23 May 2011||REMI||Maintenance fee reminder mailed|
|16 Oct 2011||LAPS||Lapse for failure to pay maintenance fees|
|6 Dic 2011||FP||Expired due to failure to pay maintenance fee|
Effective date: 20111016